Canonical Allele Identifier: CA1095883593
Gene:

Linked Data

dbSNP Id: rs1777187558

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633620A>G , CM000668.2:g.151633620A>G GRCh38
NC_000006.11:g.151954755A>G , CM000668.1:g.151954755A>G GRCh37
NC_000006.10:g.151996448A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3638A>G